COPD, Chronic Obstructive Pulmonary Disease Clinical Trial
Official title:
Home-based Pulmonary Rehabilitation for COPD Patients
Objectives The objective of this project is to motivate patients with COPD to incorporate the habit of doing daily mindful physical activity by using the proposed home-based pulmonary rehabilitation program that integrates video guided exercises, activity monitoring daily steps and health coaching. This program will allow patients to complete Pulmonary Rehabilitation (PR) at home and promote behavior change and lead to a more active lifestyle for patients with COPD who have been prescribed PR. The program will be able to effectively monitor daily step count. A health coach will receive more this detailed data and will guide weekly health coaching sessions designed to increase awareness of the physical activities completed and ignite inner motivation for healthy behaviors. The proposed PR program is innovative and responds to an unmet need in chronic care for COPD patients in the context of COVID-19 pandemic and it mitigates the common accessibility barriers.
| Status | Not yet recruiting |
| Enrollment | 80 |
| Est. completion date | December 2028 |
| Est. primary completion date | December 2027 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 40 Years to 100 Years |
| Eligibility | Inclusion Criteria: - Men and women age 40 years and older - FEV1 <80% or less (forced expiratory volume in one second) as documented by pulmonary function. - Medical diagnosis of COPD, GOLD classification B,D, and C based on symptoms and history of exacerbations. - The patients must be able to access a smart-phone or computer tablet with internet service. Exclusion Criteria: - Unable to perform low intensity exercise. - Patients with a high likelihood of being lost to follow-up or contact (patients with active chemical dependency), are planning to move, are not living in the healthcare area. - Patients with an inability to provide good data or follow commands (patients who are disoriented, have a severe neurologic or psychiatric condition). |
| Country | Name | City | State |
|---|---|---|---|
| Sweden | Karolinska Institutet | Stockholm |
| Lead Sponsor | Collaborator |
|---|---|
| Karolinska Institutet |
Sweden,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Disease specific quality of life | Chronic Respiratory Questionnaire (CRQ) | 8-12 weeks | |
| Primary | Modified Medical Research Council Dyspnea scale (mMRC), | Dyspnea | 8-12 weeks | |
| Primary | COPD assessment Test (CAT) | assess symptoms of breathing | 8-12 weeks | |
| Secondary | GAD to asses anxiety and depression symptoms | assessing anxiety and depression symptoms | 8-12 weeks | |
| Secondary | Online breathing and mindful movement exercises/ exercise routine | Total time performing the breathing exercises | 8-12 weeks | |
| Secondary | Activity monitoring | number of steps | 8-12 weeks |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT05016466 -
GOLD 0 - DLCO 1: A Look Beyond the Obstruction. Is Spirometry Enough for COPD (Chronic Obstructive Pulmonary Disease) Screening?
|
||
| Not yet recruiting |
NCT05114434 -
Effect of BDP/Formoterol/G on Cough Efficacy in Moderate to Severe COPD Patients (EFFICACE)
|
||
| Recruiting |
NCT05297279 -
OMEGA - Dietary Intervention - COPD Trial
|
N/A | |
| Recruiting |
NCT03658538 -
Motivational Interviewing and Air Cleaners for Smokers With COPD (MOVE COPD)
|
N/A | |
| Completed |
NCT02937584 -
A Study to Assess the Effects of PT001 and PT005 MDI on Specific Image Based Parameters in Subjects With Moderate to Severe COPD
|
Phase 3 |